All recall categories

Recalls distributed in Arizona

These notices name Arizona in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,043 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Arizona too — those are in the archive.

Food

Reported Apr 8, 2015

Granny Smith Apples, "Granny's Best" or "Big B"; sold in 40-45 lb. cases with cardboard trays or in 3 lb. poly bags…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bidart Bros.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

Austin Grand Prize Green Salsa; 1st Runner-up Texas Hot Sauce Challenge 1992; Mfg. Exclusively for: Skins N More Inc.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Creative Foodworks, Inc.

51 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2015

Horchata Post Mix Fountain Syrup, 3 gallons (11.4 Liters), UPC 0 09319 00006 0.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fiesta Pacific Products Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2015

Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc. Cardiac Rhythm Disease Management

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

The package reads in part "***Northern Chef***GLUTEN FREE, OVEN READY LIGHTLY COATED COD***KEEP FROZEN/DO NOT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tai Foong U.S.A., Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2015

Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgical…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ArthroCare Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2015

Diamondback 360 Coronary Orbital Atherectomy System, Model Number: DBEC-125. The system is indicated to facilitate…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cardiovascular Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2015

Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

fgf brands, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 1, 2015

Stonewall Kitchen Buffalo Wing Sauce Net Wt. 17.5 oz. glass jar UPC 711381-31395 4 Item # 251805,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2015

Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Titan Spine, LLC

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2015

Natural Grocers brand Organic Garlic Powder. Natural Grocers brand Organic Garlic Powder. Packaged in Zip-Lock-type…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Vitamin Cottage Natural Food Markets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2015

Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

St Jude Medical

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 23, 2015

Stock Yards Meat Packing Co., Inc. Retira Producto De Carne Asada (Roast Beef) Debido A Un Posible Error De Rotulacin

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Recalling firm not stated

USDA FSIS

Medical devices

Reported Mar 18, 2015

Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB), 8 Fr 40 cc Model: IAB-05840-LWS

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microport Orthopedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pivotal Health Solutions

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.